When Victoria Garcia learned midway through her pregnancy that her daughter Julia would be born with Achondroplasia, her world shifted—but her purpose became clearer than ever. As a neonatal nurse and mother of two, Victoria brings a unique blend of personal and...
In this heartfelt episode of Child Life On Call, host Katie Taylor speaks with Kate, a devoted mom, advocate, and founder of Brave Bears Club. Kate shares her powerful journey navigating her daughter Charlotte’s diagnosis of infantile spasms—a rare and devastating...
On this week’s episode, Katie wraps up the year with, Lyndsey (CLOC admin + podcast editor) sharing about what the common themes across the episodes were in 2022. This year was a memorable one as there were so many parents who so candidly shared their story on...
Being close to a trusted adult is powerful. It lessens pain and brings comfort when kids need it most. This guide shows you how to keep kids safe, and help them feel supported, during medical procedures. From the Meg Foundation for Pain and Child Life On Call.
![264: An Unexpected Diagnosis at 22 Months: Infantile Spasms and Advocacy [REPOST] -Kate’s Story](https://childlifeoncall.com/wp-content/uploads/2025/07/Family_Ten_BCHT_February_2025-20-1-1080x675.jpg)
